Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/66—Polyesters containing oxygen in the form of ether groups
  • C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/672—Dicarboxylic acids and dihydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
  • C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
  • C08J3/07—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
  • C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/04—Coating
  • C08J7/0427—Coating with only one layer of a composition containing a polymer binder
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/60—Optical bleaching or brightening
  • D06L4/671—Optical brightening assistants, e.g. enhancers or boosters
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/507—Polyesters
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/507—Polyesters
  • D06M15/5075—Polyesters containing sulfonic groups
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
  • D06P1/0004—General aspects of dyeing
  • D06P1/0016—Dye baths containing a dyeing agent in a special form such as for instance in melted or solid form, as a floating film or gel, spray or aerosol, or atomised dyes
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
  • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
  • D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
  • D06P1/5264—Macromolecular compounds obtained otherwise than by reactions involving only unsaturated carbon-to-carbon bonds
  • D06P1/5271—Polyesters; Polycarbonates; Alkyd resins
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
  • D06P3/34—Material containing ester groups
  • D06P3/52—Polyesters
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
  • C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31786—Of polyester [e.g., alkyd, etc.]
  • Y10T428/31797—Next to addition polymer from unsaturated monomers

Definitions

• a process for providing a shaped article made from an essentially linear crystallizable polyester with a durable, modified surface comprising treating the shaped article with a water-insoluble crystallizable polymeric compound, said polymeric compound being characterized in that (A) it has a crystalline melting point above 100 C., measured by the temperature of disappearance of birefringence, (B) it contains crystallizable segments of repeat units identical with the repeat units forming the crystallizable portions of the polyester shaped article, and (C) it contains at least one active group serving to modify the surface of the shaped article, the said active group being selected from at least one of the following: an acidic group, a basic group, an ionisable salt group, a water-solvatable polymeric group, an anti-oxidant group, a group which absorbs ultra-violet light of wavelength 290-400 mg and dissipates it in a manner harmless to the shaped article, a group which contains siliconor fluor
• the present invention relates to a surface-modifying treatment of shaped articles, such as filaments, fibres, fabrics, films and the like, made from synthetic crystallisable polyesters.
• Polyesters because of their relatively nonpolar nature, do not develop very high forces with agents for surface-treatment in this second way, consequently it has proved difficult to carry out a surface treatment of polyesters to obtain an effect which is permanent and very resistant towards washing, scouring, dry-cleaning, and other processes to which the derived articles may be subjected.
• a particular advantage of such a reduction in treating temperature is that the surface of a polyester shaped article may now be given a durable modification by treatment in an aqueous dispersion containing a crystallisable polymeric compound and a swelling agent, without the necessity for a separate high temperature baking operation. Fabrics derived from bulked polyester yarns which cannot be heated to high temperatures may therefore now also be given a more durable surface treatment by the present process.
• a process for providing a shaped article made from an essentially linear crystallisable polyester with a durable, modified surface comprising treating the shaped article with a water-insoluble crystallisable polymeric compound, said polymeric compound being characterised in that (A) is has a crystalline melting point above C., measured by the temperature of disappearance of birefringence, (B) it contains crystallisable segments of repeat units identical with the repeat units forming the crystallisable portions of the polyester shaped article, and (C) it contains at least one active group serving to modify the surface of the shaped article, the said active group being selected from at least one of the following: an acidic group, a basic group, an ionisable salt group, a water-solvatable polymeric group as defined, an antioxidant group, a group which absorbs ultra-violet light of wavelength 290400 III/L and dissipates it in a manner harmless to the shaped article, a group which contains siliconor fluorine-based water-re
• a stable dispersion of a copolymer solution in water said copolymer solution comprising a block or graft copolymer, containing crystalline polyester segments and polyoxyethylene segments, dissolved in one or more solvents of which at least one is a swelling agent for polyesters in their oriented crystalline form.
• Suitable crystallisable polymeric compounds for the treatment are those given in copending application 370,068.
• the shaped article may contain other materials, besides the polyester, for example it may be a fabric blend of oriented crystalline polyester fibres with cotton or wool fibres.
• Essentially linear crystallisable polyesters which may be treated according to our invention include fibreand filmforming polyesters and cop'olyesters derived from poly (ethylene terephthalate), poly(tetramethylene terephthalate), poly(l,4 bis-methylenecyclohexane terephthalate), poly(ethylene naphthalene-2,6-dicarboxylate), and poly (ethylene diphenoxyethane-4,4-dicarboxylate).
• poly(ethylene terephthalate) the crystallisable repeat unit has the structure and in copolyesters containing ethylene terephthalate units the crystalisable repeat unit is the same provided that the proportion of ethylene terephthalate units is high enough.
• Polyesters and copolyesters containing at least 80 mole percent of poly(ethylene terephthalate) have proved especially successful commercially.
• Particular copolymers of poly(ethylene terephthalate) which have found some industrial application and to which this process may be applied include those in which adipate, sebacate, isophthalate, or sulphoisophthalate replace terephthalate; oxydiethylene or poly(oxyethylene) replace ethylene; p-o-xyethoxybenzoate or p-oxybenzoate replace terephthalate; pentaerythritol, glycerol, or their derivatives are intro Jerusalem to form chain-branching sites; or monoalkyl poly (oxyethylene) glycol is introduced to limit chain length.
• Poly( l,4-bismethylene-cyclohexane terephthalate) has also proved successful commercially.
• essentially linear we mean that the polyester is either unbranched or exhibits a minor degree of chain branching insufficient to render the polyester insoluble in solvents which dissolve the unbranched polymer.
• the shaped polyester article is preferably treated in its oriented i.e. drawn, crystalline condition.
• the active group present in the crystallisable polymeric compound can be either simple or polymeric, and may be present as an end group in the molecule or may be attached to other groups at one or more than one position. Of course, more than one active group may be present in the molecule of the crystallisable compound, and other groups which confer neither crystallisability nor surface modification may also be present.
• the effect of incorporating an acidic group as an active group in the crystallisable polymeric compound is to render the surface of the shaped article receptive to basic materials such as basic polymers and copolymers or basic dyestuffs.
• the effect of incorporating a basic group as an active group in the crystallisable polymeric compound is to render the surface of the shaped article receptive to acidic materials, such as acidic polymers and copolymers or acid dyestuffs.
• Acidic or basic groups may be incorporated in the crystallisable polymeric compound in the form of their ionisable salts instead of as the un-neutralised acid or base.
• the acidic group or salt thereof may be a relatively weak acid or a salt of a relatively weak acid, such as a carboxylic acid, or it may be a relatively strong acid or a salt of a relatively strong acid, such as a sulphonic or phosphonic acid. Strong acids and their salts are particularly effective in modifying the surface properties of shaped articles.
• the acidic group or salt thereof may be derived from a monomeric material; thus for example the crystallisable compound may contain acidic end-groups, such as p-sulphobenzoic ester groups, or acidic difunctional groups such as 5-sulphoisophthalic ester groups.
• the acid group or salt thereof may be derived from a polymeric material, such as poly(ethylene S-sulphoisophthalate).
• the crystallisable compound may be a block or graft copolymer.
• the basic group is nitrogenous.
• the nitrogenous basic group or groups may be derived from a monomeric material; thus, for example, the crystallisable compound may contain basic endgroups, such as N,N-dimethyl hydrazide or dimethylaminoethyl ester end-groups, or basic difunctional groups such as N-methyldiethanol-amine ester groups.
• the nitrogenous basic group or groups may be derived from a polymeric material, such as polyethyleneirnine or a poly (aminotriazole), in which case the crystallisable compound may be a block or graft copolymer.
• the nitrogenous basic group or groups may contain primary, secondary, tertiary, or quaternary basic groups.
• the effect of incorporating a water-solvatable polymeric group is to render the surface of the shaped article hydrophilic and therefore Wettable by water. Soil, particularly when attached to the shaped articles by oily substances is more easily displaced by water or aqueous detergents when the surface of the shaped article is rendered more hydrophilic, and the redeposition of soil from detergent media is also reduced. As a result, treated articles are washed more easily and more effectively than untreated articles.
• a further effect of incorporating a water solvatable group is to increase the ability of adhesives, gums and sizes, including textile sizes to adhere to the shaped article surface. In the case of filament yarns such improvements in size adhesion enables the yarn to be used as weaving warps without first subjecting the yarns to a twisting operation.
• a water-solvatable polymeric group We mean a polymeric group derived from a water-soluble polymer of average molecular weight at least 300, except that in the case where the water-solvatable polymeric group is a polyoxyalkylene group, the polyoxyalkylene group is derived from a polyoxyalkylene glycol having an average molecular weight in the range 300 to 6,000 inclusive and the Viscosity Ratio of the crystallisable polymeric compound, as measured in a 1% solution in orthochlorophenol at 25 C., lies in the range of 1.1 to 1.5.
• polymeric groups derived from watersoluble polymers such as poly(vinyl alcohol), poly(vinyl methyl ether), poly(N,N-dimethyl acrylamide), methylcellulose, or hydroxyethyl cellulose are suitable for use as active groups.
• polymeric groups derived from water-soluble poly (oxyal'kylene) glycols are particularly suitable for use as active groups.
• Suitable polyoxyalkylene groups include polyoxyethylene, polyoxypropylene, polyoxytrimethyleen, polyoxytetramethylene, polyoxybutylene, and copolymers thereof.
• polyoxyethylene groups derived from polyoxyethylene glycols having an average molecular weight of 3006000 are most suitable, and we particularly prefer to use polyoxyethylene groups derived from polyoxyethylene glycols having an average molecular weight in the range 1000 to 4000 inclusive.
• polyoxyethylene groups derived from a particular polyoxyethylene glycol this does not necessarily imply the use of that particular polyoxyethylene glycol in the preparation of the crystallisable polymeric compound but means that the polyoxyethylene group together with the elements of water is equivalent in molecular weight to that particular polyoxyethylene glycol; thus for example a polyoxyethylene group with a molecular Weight of 282 is derived from a polyoxyethylene glycol of molecular weight 300.
• crystallisable polymeric compound used in the treatment should itself be capable of forming shaped articles such as fibres or films, and indeed we prefer to use a crystallisable polymeric compound which is not itself capable of forming fibres, although crystallisable polymeric compounds which are capable of forming shaped articles can be used.
• crystallisable polymeric compound which is defined by a viscosity ratio, as measured in a 1% solution in orthochlorophenol at 25 C., in the range 1.1 to 1.5. No useful fibreand film-forming properties are exhibited by the crystallisable polymeric compounds with the active groups and having viscosity ratios in this range. Crystallisable polymeric compounds having viscosity ratios above this range, although effective, are rather more difficult to disperse in aqueous media, and more diflicult to handle in solution and in the molten state, than crystallisable polymeric compounds having viscosity ratios within our range.
• our crystallisable polymeric compounds preferably contain 50% by weight of ethylene terephthalate repeat units together with 90 to 50% by weight of polyoxyethylene terephthalate repeat units derived from a polyoxyethylene glycol of average molecular weight 1000 to 4000, the molar ratio of ethylene terephthalate units to polyoxyethylene terephthalate units being between 2:1 and 6:1.
• the crystallisable polymeric compound may be a random copolymer, or it may be a block copolymer, or it may be a graft copolymer.
• the crystallisable polymeric compound will be a block or graft copolymer, and where the active group is not polymeric the crystallisable polymeric compound will usually be a random copolymer, but may alternatively be a block or graft copolymer.
• the active group is not polymeric and appears only as endgroups in the crystallisable polymeric compound, the crystallisable polymeric compound is not strictly a copolymer at all, but rather a homopolymer with active endgroups.
• Suitable swelling agents are selected by their ability to induce crystallisation in transparent amorphous polymer films made from the fibre-forming polyester.
• a compound suitable as a swelling agent for poly- (ethylene terephthalate) shaped articles at a given temperature can 'be observed visually to induce crystallisation in transparent amorphous poly(ethylene terephthalate) film when it is treated with the compound at the given temperature.
• Examples of compounds which are suitable in this invention as swelling agents for polyester shaped articles include benzaldehyde, benzyl alcohol, methyl salicylate, chloroform, trichloroethylene, o-dichlorobenzene, dimethyl phthalate, methylene chloride, diethyl oxalate, diethyl succinate, methyl iodide, tetrachloroethane, o-phenylphenol, l-phenylethanol.
• Preferred swelling agents are o-phenylphenol, l-phenylethanol, methyl salicylate and benzyl alcohol.
• a suitable ratio of the weight of the crystallisable polymeric compound to the weight of the swelling agent is within the range 2:98 to 95:5.
• the swelling agent acts as a dyeing assistant a separate dye carried may not be required.
• the aqueous dispersion of the crystallisable polymeric compound and the swelling agent may be added to the dyebath; however, since the presence of certain dyestuffs at high concentration appears sometimes to interfere with the surface treatment it is sometimes preferable to add the aqueous dispersion at a later stage, that is, when the concentration of dyestufr in the bath is low due to exhaustion on to the polyester shaped article.
• the aqueous dispersion be stabilised by the use of at least one dispersing or surface active agent.
• dispersing agents are suitable for stabilising the aqueous dispersion of the crystallisable polymeric compound and the swelling agent at high temperatures. These include sodium salts of sulphonated castor oils, sodium salts of sulphonated alkyene naphthalenes, or dispersing agents based on alkyl ether phosphates.
• Protective colloids such as gelatine are also useful.
• EXAMPLE 1 This example illustrates a durable surface treatment of a fabric woven from poly(ethylene terephthalate) filament yarn wherein the treatment is carried out at room temperature and at 60 C. wtih a solution of a crystallisable polymeric compound in benzyl alcohol as the swelling agent for poly(ethylene terephthalate) drawn filament yarn.
• Dimethyl terephthalate (194 parts) ethylene glycol parts, poly (oxyethylene) glycol of average molecular weight 1540 (440 parts), 2,6-di-tert-butyl-4-methyl phenol (0.44 part), calcium acetate (0.1512 part) and antimony trioxide (0.0388 part) were heated from 194 C. to 234 C. over a period of 4 /2 hours during which time 57 parts of methanol were removed by distillation.
• Phosphorous acid (0.141 part of a 24.8% solution in ethylene glycol) was added and the molten material was transferred to a polymerization tube heated to 282 C. After the excess glycol had been blown off in a rapid stream of nitrogen the pressure was reduced to 0.1 mm.
• a solution of 20% of this compound in benzyl alcohol was used as a padding bath in which 100% poly (ethylene terephthalate) taffeta fabric was immersed for 2 minutes; the temperature of the padding bath being maintained at room temperature for one fabric sample and at 60 C. for a second fabric sample.
• the fabrics were then drained of excess solution and rinsed in a mixture of acetone (10 parts) and water (90 parts) followed by rinsing in water.
• the fabrics were finally dried in a hot air tumble drier at 60 C.
• the lengthwise resistances of 7" x 1 /2 samples of treated and untreated fabrics were measured at 65% relative humidity.
• the treated fabrics were then subjected to a series of 80 wash-dry cycles, each consisting of a 6 minute wash in a 0.07% solution of a commercial soap powder at 60 C. in a domestic washing machine, rinsing in water, 3 spin-dry treatments, and drying in a hot air tumble drier at 60 C.
• the fabrics were rinsed in water of conductivity 1.5 x l mho, spin dried for 2 minutes, and tumble dried at 60 C.
• the lengthwise electrical resistances of samples 7" X 1 /2" were measured at 65% relative humidity. The following results were obtained.
• Example 1 The compound, prepared as described in Example 1, was dissolved in benzaldehyde to give a 10% solution. 10 parts by volume of this solution were dispersed in 190 parts by volume of water and the resulting emulsion used as a padding bath in which a 100% poly(ethylene terephthalate) taffeta fabric was treated for /2 minute at a padding bath temperature of 60 C. The fabric was then drained, rinsed, and dried as described in Example 1. The treated fabric, subjected to 40 wash-dry cycles as described in Example 1, developed no appreciably stable electrostatic charge when rubbed and was accordingly resistant to soiling. The treated, washed fabric was also readily wetted by water, and oil was readily displaced from the fabric by water.
• the treated fabric so subjected to 40 wash-dry cycles and conditioned as described in Example 1, had a lengthwise (7" x 1 /2" sample) electrical resistance of 2.8)(10 megohms compared with 10 megohms for untreated fabric.
• EXAMPLE 3 This is a comparative example which illustrates that the surface treatment of poly (ethylene terephthalate) fabric is not durable when treatment is carried out at 60 C. with an aqueous dispersion of a crystallisable polymeric compound dissolved in ethyl benzoate which is a poor swelling agent for poly(ethylene terephthalate), but is durable when a good swelling agent, in this case 0- phenylphenol, is added to the aqueous dispersion.
• a padding bath was prepared from 100 parts of an emulsion as prepared in section (i) of this example to which were added 0.5 part of the sodium salt of ophenyl phenol and 1 part of glacial acetic acid.
• a poly(ethylene terephthalate) taffeta fabric was treated with this padding bath and examined as described in Section (i) of this example except that the treated fabric was subjected to 40 wash-dry cycles.
• the washed, treated fabric had a lengthwise (7" X 1 /2" sample) electrical resistance of 2.3)(10 megohms, and when rubbed against another 100% poly(ethylene terephthalate) fabric developed no appreciably stable electrostatic charge and was accordingly resistant to soiling.
• the treated washed fabric was also wetted by water, and oil was readily removed from the fabric by water.
• EXAMPLE 4 This illustrates the durable treatment of fabric comprising poly(1,4bismethylene cyclohexane terephthalate) fibres and wool using a crystallisable polymeric compound in which the crystallisability is due to 1,4-bismethylenecyclohexane terephthalate units, and the comparative example illustrates that the treatment is not effective using a crystallisable polymeric compound in which the crystallisability is due to ethylene terephthalate units. Both examples illustrate treatment at 60 C. in presence of chloroform which is a good swelling agent for poly(1,4-bismethylenecyclohexane terephthalate).
• Dimethyl terephthalate (97 parts), 1,4-bishydroxymethyl cyclohexane (51.5 parts), poly(oxyethylene) glycol of average molecular weight 1540 (220 parts), and tetra-butyl titanate (0.074 part) were heated under atmospheric pressure 272 C. until the theroretical volume of methanol had been evolved.
• the resultant product (viscosity ratio 1.16 as measured on a 1% solution in orthochlorophenol at 25 C.) melted (as shown by final loss of birefringence) at 248 C.
• the product was dissolved in chloroform to give a 10% solution.
• a woven fabric comprising 55% poly(1,4-bismethylenecyclohexane terephthalate) and 45% wool was treated with this solution by the method described in Example 1 except using treating conditions of 60 C. for 10 minutes.
• COMPARATIVE EXAMPLE 4A The compound, prepared as described in Example 1, was dissolved in chloroform to give a 10% solution.
• the fabric was difficult to wet by water and soiled in the same way as untreated fabric, thus illustrating that, even in the presence of a good swelling agent, the treatment is not effective when the repeating units causing crystallinity in the compound used for the treatment (in this case, ethylene terephthalate units) are not the same as the units producing crystallinity in the article treated (in this case, 1,4-bismethylenecyclohexane terephthalate units).
• EXAMPLE 5 This example illustrates a durable surface treatment of a 100% poly(ethylene terephthalate) fabric wherein the treatment is carried out during dyeing at C. using a dyebath additive comprising an aqueous dispersion of a solution of a poly(ethylene terephthalate)poly(oxyethylene) terephthalate copolymer in l-phenylethanol.
• the compound, prepared as described in Example 1, was dissolved in l-phenyl ethanol to give a 40% solution. To parts of this solution were added 32 parts of an 83% aqueous solution of Turkey Red Oil. The resulting composition, heated to 50 C., was added with stirring to a solution of gelatine (16 parts) in water (212 parts) also at 50 C. The resulting dispersion was passed through a Manton-Gaulin homogeniser then stirred until cool.
• a dyebath was prepared by adding 0.33 part of Cl. Disperse Blue 26, 0.075 part of the disodium salt of methylene dinaphthalene sulphonic acid as a 25% aqueous solution, and 3 parts of the dispersion prepared as above to 100 parts of water.
• a 100% poly(ethylene terephthaate) plain weave fabric was dyed at 130 C. for 1 hour in the above dyebath using a liquor ratio of 30:1.
• the treated, washed fabric was also readily wetted by water, and oil was readily displaced from the fabric by water.
• the treated fabric so subjected to 40 wash-dry cycles and conditioned as described in Example 1, had a lengthwise (7" x 1 /2" sample) electrical resistance of 6.6)( megohms compared with 5.5 10 megohms for untreated dyed fabric.
• EXAMPLE 6 This example illustrated a durable surface treatment of a fabric derived from a bulked poly(ethylene terephthalate) yarn wherein the treatment is carried out at 95 C. by adding an aqueous dispersion of a solution of a poly(ethylene terephthalate)poly(oxyethylene) terephthalate copolymer in l-phenylethanol to a dyebath subsequent to the dyeing process.
• a dyebath was prepared by adding 0.035 part of Cl. Disperse Blue 56, 0.075 part of the disodium salt of methylene dinaphthalene sulphonic acid (as a aqueous solution), and 0.5 part of a aqueous solution of acetic acid to 100 parts of water.
• a fabric knitted from a stabilised false twist crimped poly(ethylene terephthalate) yarn was placed in the dyebath using a liquor ratio of 30:1.
• the dyebath was now heated to 95 C. and 0.35 part of the sodium salt of o-phenyl phenol, dissolved in a small volume of water, were added during a period of 20 minutes. The temperature of the bath was maintained at 95 C.
• the treated fabric so subjected to 20 wash-dry cycles and conditioned as described in Example 1, had a lengthwise (7" x 1 /2 sample) electrical resistance of 5.7 10 megohms compared with 5 X 10 megohms for untreated, dyed fabric.
• EXAMPLE 7 This example illustrates a durable surface treatment of biaxially orientated poly(ethylene terephthalate) film to render it antistatic and thus to reduce its propensity for attracting dust.
• the compound, prepared as described in Example 1, was dissolved in chloroform to give a 10% solution.
• the solution was used as a treating bath in which a strip of biaxially oriented poly(ethylene terephthalate) film was immersed for 5 minutes at C. the treated film, even after scouring in 0.07% Persil solution at C. for 1 hour, developed no appreciably stable electrostatic charge when rubbed and accordingly did not attract dust.
• EXAMPLE 8 This example illustrates the treatment of a poly(ethylene terephthalate) monofilament to render its surface hydrophilic.
• the compound, prepared as described in Example 1, was dissolved in benzyl alcohol to give a 15% solution.
• This solution was used as a treating bath in which a length of poly(ethylene terephthalate) monofilament of diameter 0.006 inch was immersed for 3 minutes at 60 C.
• the treated monofilament was washed in 20% aqueous methanol then dried in a current of warm air.
• a process for providing a shaped article made from an essentially linear crystallizable polyester with a. durable modified surface comprising contacting the shaped article at a temperature between room temperature and 140 C. with a composition consisting essentially of a water-insoluble crystallizable polymeric compound, said polymeric compound (A) haivng a crystalline melting point above C., measured by the temperature of disappearance of birefringence, (B) containing crystallizable segments of repeat units identical with the repeat units forming the crystallizable portions of the polyester shaped article, and (C) containing at least one active group serving to modify the surface of the shaped article, the said active group being: an acidic group, a basic group, an ionizable salt group, a water-solvatable polymeric group of average molecular weight at least 300, an anti-oxidant group, a group which absorbs ultra-violet light of wavelength 290-400 III/.0 and dissipates it in a manner harmless to the shaped article, a group which contains siliconor
• crystallisable polyester segments of repeat units in the crystallisable polymeric compound are poly(ethylene terephthalate) segments.
• crystallisable polyester segments of repeat units in the crystallisable polymeric compound are poly(1,4-bismethylenecyclohexane terephthalate) segments.
• crystallisable polyester segments of repeat units in the crystallisable polymeric compound are poly(ethylene-1,2-diphenoxyethane-4,4'-dicarboxylate) segments.
• the crystallizable polymeric compound contains at least one active group which is an acidic group selected from the group consisting of carboxylic acid, sulphonic acid, and phosphonic acid groups and salts of the said acids, which are compatible with the swelling agent.
• At least one active group is a water-solvatable polyoxyalkylene group selected from the group consisting of polyoxyethylene, polyoxypropylene, and copolymers thereof.
• polyoxyethylene group is derived from a polyoxyethylene glycol having an average molecular weight between 1,000 and 4,000 inclusive.

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• Textile Engineering (AREA)
• Medicinal Chemistry (AREA)
• Organic Chemistry (AREA)
• Polymers & Plastics (AREA)
• Health & Medical Sciences (AREA)
• Dispersion Chemistry (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Coloring (AREA)
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• 1964
  • 1964-07-22 GB GB29580/64A patent/GB1118875A/en not_active Expired
  • 1964-07-22 GB GB55967/67A patent/GB1119368A/en not_active Expired
  • 1964-07-22 GB GB29581/64A patent/GB1119367A/en not_active Expired
• 1965
  • 1965-06-28 US US467745A patent/US3479212A/en not_active Expired - Lifetime
  • 1965-07-15 DE DE19651719547 patent/DE1719547B2/de active Granted
  • 1965-07-16 DK DK366565AA patent/DK118427B/da unknown
  • 1965-07-21 NL NL6509456A patent/NL6509456A/xx unknown
  • 1965-07-21 ES ES0315632A patent/ES315632A1/es not_active Expired
  • 1965-07-21 CH CH1025165D patent/CH1025165A4/xx unknown
  • 1965-07-21 SE SE9631/65A patent/SE312115B/xx unknown
  • 1965-07-21 CH CH1025165A patent/CH501768A/de not_active IP Right Cessation
  • 1965-07-22 BE BE667248A patent/BE667248A/xx unknown
  • 1965-07-22 LU LU49148A patent/LU49148A1/xx unknown
  • 1965-07-22 FR FR25668A patent/FR1455242A/fr not_active Expired
  • 1965-07-22 BE BE667249A patent/BE667249A/xx unknown
  • 1965-07-22 AT AT676565A patent/AT267041B/de active

Patent Citations (7)

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